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International Regulatory Affairs Lead - Submissions & Strategy

Job in Salisbury, Wiltshire, SP1, England, UK
Listing for: KalVista Pharmaceuticals
Full Time position
Listed on 2026-01-06
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
  • Management
    Healthcare Management
Job Description & How to Apply Below
A global pharmaceutical company is seeking an Associate Director of Regulatory Affairs to lead regulatory compliance for international markets. The role includes managing regulatory submissions, representing the regulatory team in launch activities, and collaborating across various functions. Candidates should have a BSc in relevant sciences and at least 10 years in Regulatory Affairs, with strong communication and project management skills.
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